Canonical Allele Identifier: CA288166693

Gene: NCOR1 TTC19

Linked Data

• dbSNP Id: rs895716360
• gnomAD v2: 17-15932636-A-G
• gnomAD v3: 17-16029322-A-G
• gnomAD v4: 17-16029322-A-G
• MyVariant Identifiers: chr17:g.15932636A>G (hg19) ; chr17:g.16029322A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16029322A>G , CM000679.2:g.16029322A>G	GRCh38
NC_000017.10:g.15932636A>G , CM000679.1:g.15932636A>G	GRCh37
NC_000017.9:g.15873361A>G	NCBI36
NG_029806.1:g.34943A>G
NG_047111.1:g.192425T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436068.2:c.*2974T>C (NCOR1)	ENSP00000389839.2:n.*2974T>C
ENST00000704743.1:n.9245T>C (NCOR1)
ENST00000704744.1:c.*2974T>C (NCOR1)	ENSP00000516021.1:n.*2974T>C
ENST00000704745.1:c.*2974T>C (NCOR1)	ENSP00000516022.1:n.*2974T>C
ENST00000261647.10:c.*1800A>G (TTC19) MANE Select	ENSP00000261647.5:n.*1800A>G
ENST00000268712.8:c.*2974T>C (NCOR1) MANE Select	ENSP00000268712.2:n.*2974T>C
ENST00000268712.7:c.*2974T>C (NCOR1)	ENSP00000268712.2:n.*2974T>C
ENST00000470649.1:c.247+2620A>G (TTC19)	ENSP00000465627.1:n.247+2620A>G
NM_001271420.1:c.*1800A>G (TTC19)	NP_001258349.1:n.*1800A>G
NM_017775.3:c.*1800A>G (TTC19)	NP_060245.3:n.*1800A>G
XM_017024801.2:c.994+2620A>G (TTC19)	XP_016880290.2:n.994+2620A>G
XM_017024802.2:c.994+2620A>G (TTC19)	XP_016880291.2:n.994+2620A>G
NM_006311.4:c.*2974T>C (NCOR1) MANE Select	NP_006302.2:n.*2974T>C
NM_017775.4:c.*1800A>G (TTC19) MANE Select	NP_060245.3:n.*1800A>G
NM_001271420.2:c.*1800A>G (TTC19)	NP_001258349.1:n.*1800A>G